NDCFind

Cyclobenzaprine Hydrochloride 71205-0678

Product NDC

71205-0678
Manufacturer
Proficient Rx Lp
Dosage Form
Tablet, Film Coated
Route
Oral
Product Type
Human Prescription Drug
Marketing Start
September 26, 2008
Listing Expires
December 31, 2026
Application
ANDA078643
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Active Ingredients

IngredientStrength
Cyclobenzaprine Hydrochloride5 mg/1

Drug Class

Centrally-mediated Muscle Relaxation [PE]Muscle Relaxant [EPC]

Packaging Options(3)

30 TABLET, FILM COATED in 1 BOTTLE (71205-678-30)

60 TABLET, FILM COATED in 1 BOTTLE (71205-678-60)

90 TABLET, FILM COATED in 1 BOTTLE (71205-678-90)